Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Systems, Data ... Experience with Rave Medidata or similar EDC platforms * Experience integrating IxRS and EDC ...
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Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Systems, Data ... Experience with Rave Medidata or similar EDC platforms * Experience integrating IxRS and EDC ...
Medidata Rave Programmer information
See California salary details
$11.86 - $16.95
4% of jobs
$16.95 - $22.04
9% of jobs
$25.70 is the 25th percentile. Wages below this are outliers.
$22.04 - $27.13
17% of jobs
$27.13 - $32.22
13% of jobs
The median wage is $35.19 / hr.
$32.22 - $37.31
13% of jobs
$37.31 - $42.40
10% of jobs
$42.40 - $47.49
9% of jobs
$48.44 is the 75th percentile. Wages above this are outliers.
$47.49 - $52.58
9% of jobs
$52.58 - $57.67
7% of jobs
$57.67 - $62.76
6% of jobs
$62.76 - $67.85
4% of jobs
$11
$39
$67
How much do medidata rave programmer jobs pay per hour?
As of May 29, 2026, the average hourly pay for medidata rave programmer in California is $39.02, according to ZipRecruiter salary data. Most workers in this role earn between $25.38 and $50.77 per hour, depending on experience, location, and employer.
What is a Medidata Rave Programmer job?
A Medidata Rave Programmer is responsible for designing, developing, and managing electronic data capture (EDC) systems using Medidata Rave, a widely used clinical trial software. They create study databases, build edit checks, program custom functions, and ensure data integrity for clinical trials. Their role is essential in streamlining data collection, validation, and reporting for regulatory compliance and efficient trial management.
What are the key skills and qualifications needed to thrive in the Medidata Rave Programmer position, and why are they important?
To thrive as a Medidata Rave Programmer, you need strong programming skills, experience in electronic data capture (EDC) for clinical trials, and a background in life sciences or a related field. Expertise with Medidata Rave software, familiarity with Rave Architect, and knowledge of relevant clinical data standards or CDISC certification are highly valuable. Attention to detail, effective communication, and problem-solving abilities help you excel in both independent and collaborative environments. These skills and qualities ensure accurate database builds, smooth study execution, and successful teamwork within clinical research settings.
What are some typical daily tasks for a Medidata Rave Programmer?
As a Medidata Rave Programmer, your daily tasks often involve designing and programming electronic case report forms (eCRFs), managing edit checks, and customizing the study database in the Medidata Rave platform. You'll collaborate closely with clinical data managers, biostatisticians, and other stakeholders to ensure accurate data capture and compliance with study protocols. Routine responsibilities may also include troubleshooting technical issues, validating builds, and supporting user testing. This role offers a balance of independent programming work and teamwork, providing opportunities to contribute directly to successful clinical trials.
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Contractor
Posted 17 days ago
Job description
Job Title: Clinical Systems Leader (CSL)
Location: South San Francisco, CA
Work Model: Hybrid (Tuesday–Thursday onsite; 2 days remote)
Interview Process: 2 Rounds (1 Virtual, 1 Onsite)
Experience Required: 2–5 Years
Overview
The Clinical Systems Leader (CSL) is responsible for the implementation and oversight of clinical technology systems supporting Early Clinical Development (ECD) trials (Phase 1–1B/2). This role focuses on system build, vendor management, protocol interpretation, and technical oversight of IxRS/IRT and eCOA systems.
The CSL works cross-functionally with Clinical Operations, Data Management, Biostatistics, Drug Supply Chain, Procurement, and external technology vendors to ensure clinical systems are built, deployed, and maintained in alignment with study protocols and regulatory requirements.
This is not a people management role. The position reports within the Clinical Insights Group and supports early-phase clinical studies.
Key Responsibilities
Study Execution & System Management
- Lead implementation of clinical systems including IxRS/IRT and eCOA/ePRO
- Oversee system builds for early-phase clinical studies
- Ensure systems align with protocol requirements and operational strategy
Project & Vendor Management
- Manage timelines and deliverables for study-related system builds
- Interpret clinical study protocols and translate into technical system requirements
- Lead vendor selection and oversee vendor deliverables
- Finalize system specifications and ensure successful deployment
Technical Oversight
- Provide oversight of system build, configuration, validation, and maintenance
- Ensure compliance with GCP, FDA regulations, and industry best practices
- Provide oversight of UAT activities (testing execution may be external)
Issue & Risk Management
- Identify system risks and issues proactively
- Track and resolve vendor-related system issues
- Document risks, mitigation plans, and compliance documentation
Cross-Functional Collaboration
- Partner with Clinical Trial Leaders, Biostatisticians, Data Management, Drug Supply Chain, and Procurement
- Work independently with minimal oversight
- Share knowledge across the ECD team
Required Qualifications
- Bachelor’s degree in Life Sciences, Computer Science, Engineering, Information Systems, Data Science, or related field
- 2–5 years of experience in Clinical Operations or Clinical Systems Management
- 2–5 years of hands-on experience with IxRS/IRT and clinical systems
- Experience implementing IxRS/IRT, ePRO, and eCOA systems
- Strong project management and vendor oversight experience
- Working knowledge of Good Clinical Practices (GCP) and FDA regulations
- Experience documenting within regulated environments
- Strong written and verbal communication skills
Preferred Qualifications
- Experience supporting early-phase (Phase 1–1B/2) clinical trials
- Experience with Rave Medidata or similar EDC platforms
- Experience integrating IxRS and EDC systems
- Vendor-side experience (highly valued)
- Experience using Veeva
About Infobahn Softworld
Sourced by ZipRecruiter
Formed in 1996, Infobahn Softworld is a leading Technology and Professional Services Company. For many years we have successfully served the technology needs of several customers from diverse industries and locations throughout North America. Infobahn Softworld has a reputation for addressing its clients’ complex challenges with business understanding and innovative technical solutions. Infobahn specializes in full lifecycle project efforts conducted in strategic partnership with some of the world’s most prominent companies.
Industry
Recruiting and staffing services
Company size
201 - 500 Employees
Headquarters location
San Jose, CA, US
Year founded
1996